WO2014094062A1 - Procédé de production d'un réactif dans un instrument - Google Patents

Procédé de production d'un réactif dans un instrument Download PDF

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Publication number
WO2014094062A1
WO2014094062A1 PCT/AU2013/001499 AU2013001499W WO2014094062A1 WO 2014094062 A1 WO2014094062 A1 WO 2014094062A1 AU 2013001499 W AU2013001499 W AU 2013001499W WO 2014094062 A1 WO2014094062 A1 WO 2014094062A1
Authority
WO
WIPO (PCT)
Prior art keywords
instrument
concentrate
diluent
reagent
mixing
Prior art date
Application number
PCT/AU2013/001499
Other languages
English (en)
Inventor
Stephen John BAGNATO
Original Assignee
Leica Biosystems Melbourne Pty Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Leica Biosystems Melbourne Pty Ltd filed Critical Leica Biosystems Melbourne Pty Ltd
Priority to EP13865320.9A priority Critical patent/EP2934730B1/fr
Priority to US14/653,956 priority patent/US20150343445A1/en
Publication of WO2014094062A1 publication Critical patent/WO2014094062A1/fr
Priority to US17/066,094 priority patent/US20210121884A1/en

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Classifications

    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01L—CHEMICAL OR PHYSICAL LABORATORY APPARATUS FOR GENERAL USE
    • B01L3/00—Containers or dishes for laboratory use, e.g. laboratory glassware; Droppers
    • B01L3/52—Containers specially adapted for storing or dispensing a reagent
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01F—MIXING, e.g. DISSOLVING, EMULSIFYING OR DISPERSING
    • B01F23/00—Mixing according to the phases to be mixed, e.g. dispersing or emulsifying
    • B01F23/40—Mixing liquids with liquids; Emulsifying
    • B01F23/45—Mixing liquids with liquids; Emulsifying using flow mixing
    • B01F23/451—Mixing liquids with liquids; Emulsifying using flow mixing by injecting one liquid into another
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01F—MIXING, e.g. DISSOLVING, EMULSIFYING OR DISPERSING
    • B01F35/00—Accessories for mixers; Auxiliary operations or auxiliary devices; Parts or details of general application
    • B01F35/80—Forming a predetermined ratio of the substances to be mixed
    • B01F35/81—Forming mixtures with changing ratios or gradients
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01L—CHEMICAL OR PHYSICAL LABORATORY APPARATUS FOR GENERAL USE
    • B01L3/00—Containers or dishes for laboratory use, e.g. laboratory glassware; Droppers
    • B01L3/52—Containers specially adapted for storing or dispensing a reagent
    • B01L3/523—Containers specially adapted for storing or dispensing a reagent with means for closing or opening
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01L—CHEMICAL OR PHYSICAL LABORATORY APPARATUS FOR GENERAL USE
    • B01L3/00—Containers or dishes for laboratory use, e.g. laboratory glassware; Droppers
    • B01L3/52—Containers specially adapted for storing or dispensing a reagent
    • B01L3/527—Containers specially adapted for storing or dispensing a reagent for a plurality of reagents
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01L—CHEMICAL OR PHYSICAL LABORATORY APPARATUS FOR GENERAL USE
    • B01L3/00—Containers or dishes for laboratory use, e.g. laboratory glassware; Droppers
    • B01L3/56—Labware specially adapted for transferring fluids
    • B01L3/563—Joints or fittings ; Separable fluid transfer means to transfer fluids between at least two containers, e.g. connectors
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01L—CHEMICAL OR PHYSICAL LABORATORY APPARATUS FOR GENERAL USE
    • B01L3/00—Containers or dishes for laboratory use, e.g. laboratory glassware; Droppers
    • B01L3/56—Labware specially adapted for transferring fluids
    • B01L3/565—Seals
    • G—PHYSICS
    • G01—MEASURING; TESTING
    • G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N1/00—Sampling; Preparing specimens for investigation
    • G01N1/28—Preparing specimens for investigation including physical details of (bio-)chemical methods covered elsewhere, e.g. G01N33/50, C12Q
    • G01N1/30—Staining; Impregnating ; Fixation; Dehydration; Multistep processes for preparing samples of tissue, cell or nucleic acid material and the like for analysis
    • G01N1/31—Apparatus therefor
    • G01N1/312—Apparatus therefor for samples mounted on planar substrates
    • G—PHYSICS
    • G01—MEASURING; TESTING
    • G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N1/00—Sampling; Preparing specimens for investigation
    • G01N1/28—Preparing specimens for investigation including physical details of (bio-)chemical methods covered elsewhere, e.g. G01N33/50, C12Q
    • G01N1/38—Diluting, dispersing or mixing samples
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01L—CHEMICAL OR PHYSICAL LABORATORY APPARATUS FOR GENERAL USE
    • B01L2200/00—Solutions for specific problems relating to chemical or physical laboratory apparatus
    • B01L2200/02—Adapting objects or devices to another
    • B01L2200/026—Fluid interfacing between devices or objects, e.g. connectors, inlet details
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01L—CHEMICAL OR PHYSICAL LABORATORY APPARATUS FOR GENERAL USE
    • B01L2200/00—Solutions for specific problems relating to chemical or physical laboratory apparatus
    • B01L2200/06—Fluid handling related problems
    • B01L2200/0605—Metering of fluids
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01L—CHEMICAL OR PHYSICAL LABORATORY APPARATUS FOR GENERAL USE
    • B01L2200/00—Solutions for specific problems relating to chemical or physical laboratory apparatus
    • B01L2200/06—Fluid handling related problems
    • B01L2200/0689—Sealing
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01L—CHEMICAL OR PHYSICAL LABORATORY APPARATUS FOR GENERAL USE
    • B01L2200/00—Solutions for specific problems relating to chemical or physical laboratory apparatus
    • B01L2200/14—Process control and prevention of errors
    • B01L2200/143—Quality control, feedback systems
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01L—CHEMICAL OR PHYSICAL LABORATORY APPARATUS FOR GENERAL USE
    • B01L2200/00—Solutions for specific problems relating to chemical or physical laboratory apparatus
    • B01L2200/16—Reagents, handling or storing thereof
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01L—CHEMICAL OR PHYSICAL LABORATORY APPARATUS FOR GENERAL USE
    • B01L2300/00—Additional constructional details
    • B01L2300/04—Closures and closing means
    • B01L2300/041—Connecting closures to device or container
    • B01L2300/044—Connecting closures to device or container pierceable, e.g. films, membranes
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01L—CHEMICAL OR PHYSICAL LABORATORY APPARATUS FOR GENERAL USE
    • B01L2300/00—Additional constructional details
    • B01L2300/04—Closures and closing means
    • B01L2300/046—Function or devices integrated in the closure
    • B01L2300/049—Valves integrated in closure
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01L—CHEMICAL OR PHYSICAL LABORATORY APPARATUS FOR GENERAL USE
    • B01L2300/00—Additional constructional details
    • B01L2300/08—Geometry, shape and general structure
    • B01L2300/0809—Geometry, shape and general structure rectangular shaped
    • B01L2300/0812—Bands; Tapes
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01L—CHEMICAL OR PHYSICAL LABORATORY APPARATUS FOR GENERAL USE
    • B01L2400/00—Moving or stopping fluids
    • B01L2400/06—Valves, specific forms thereof
    • B01L2400/0677—Valves, specific forms thereof phase change valves; Meltable, freezing, dissolvable plugs; Destructible barriers
    • B01L2400/0683—Valves, specific forms thereof phase change valves; Meltable, freezing, dissolvable plugs; Destructible barriers mechanically breaking a wall or membrane within a channel or chamber

Definitions

  • the present invention relates broadly to a method of producing a reagent on-board an instrument such as a laboratory instrument for treating a biological tissue sample with the reagent.
  • the invention also relates generally to an instrument utilising a reagent produced on-board the instrument from a mixture of a concentrate and a diluent.
  • the invention further relates broadly to a concentrate dispenser for on-board production of an instrument reagent.
  • Immunohistochemical staining and in situ nucleic acid analysis are tools used in histological diagnosis and the study of tissue morphology. Immunohistochemical staining relies on the specific binding affinity of antibodies with epitopes in tissue samples, and the increasing availability of antibodies which bind specifically with unique epitopes present only in certain types of diseased cellular tissue. Immunohistochemical staining involves a series of treatment steps conducted on a tissue sample (typically a section) mounted on a glass slide to highlight, by selective staining, certain morphological indicators of disease states.
  • Typical treatment steps include pretreatment of the tissue sample to reduce nonspecific binding, antibody treatment and incubation, enzyme labelled secondary antibody treatment and incubation, substrate reaction with the enzyme to produce a fluorophore or chromophore highlighting areas of the tissue sample having epitopes binding with the antibody, counterstaining, and the like. Between each treatment step, the tissue sample must be rinsed to remove unreacted residual reagent from the prior step. Most treatment steps involve a period of incubation typically conducted at ambient temperature of around 25 ⁇ C up to around 40° C, while cell conditioning steps are typically conducted at somewhat higher temperatures, e.g. 90 to 100 ⁇ C.
  • In-situ DNA analysis relies upon the specific binding affinity of probes (DNA binding proteins) with unique nucleotide sequences in cell or tissue samples and similarly involves a series of process steps, with a variety of reagents and process temperature requirements. Some specific reactions involve temperatures up to 120 ⁇ C to 130 ⁇ C. In these various treatment steps it is understood that no single concentration of antibody is sufficient to account for tissue variations, processing variability and tissue sample thickness. Reagents are provided in a Ready to Use (RTU) format that cannot be varied in concentration. Alternatively, concentrates are supplied and diluted to achieve a range of staining options. However, these approaches do not address increasing customer need for workflow flexibility with ease of reagent uses.
  • RTU Ready to Use
  • an instrument utilizing a reagent said instrument including:
  • a chamber adapted to contain a concentrate
  • a diluent dispenser operatively coupled to the chamber to dispense diluent for mixing with the concentrate on-board the instrument to provide the reagent at a required concentration.
  • the instrument includes one or more mixing wells located on the instrument and configured to receive the concentrate and the diluent for mixing to provide the reagent at the required concentration.
  • the mixing well is formed in a sample staining module (SSM) of the instrument. Even more preferably the mixing well is formed in a fixed or disposable cover member of the SSM. Alternately the mixing well is a dedicated mixing well formed integral with the instrument.
  • SSM sample staining module
  • the mixing wells are located adjacent one another for serial dilution of the concentrate with the diluent.
  • the instrument includes a probe having an in- line mixing chamber adapted to receive the concentrate and the diluent to provide the reagent at the required concentration.
  • the chamber is a container supplied in a sealed condition and adapted to contain a predetermined volume of the concentrate.
  • the sealed container includes a sealing membrane arranged to contain the concentrate and an inert gas.
  • the sealing membrane is designed to be at least partly removed or pierced and the container is sized for addition of diluent for mixing on-board the instrument to provide the reagent at the required concentration.
  • the chamber comprises a plurality of the sealed containers each adapted to contain a predetermined volume of the concentrate.
  • the plurality of chambers are arranged as multiple reservoirs in a blister pack.
  • the chamber is a disposable or reusable probe tip containing the concentrate and adapted to fit to a dispensing probe of the instrument.
  • a concentrate dispenser operatively coupled to an instrument for on-board provision of a reagent, said dispenser comprising packaging adapted to contain a plurality of concentrate capsules, the packaging configured to release each of the capsules for mixing with a diluent on-board the instrument to provide the reagent at the required concentration.
  • the packaging includes a stacked cartridge adapted to contain one or more columns of the plurality of concentrate capsules. In some embodiments two or more columns of the concentrate capsules are provided in the cartridge. More preferably the dispenser also comprises a reciprocating release operatively coupled to the stacked cartridge to release a lowermost of the column of capsules form the cartridge for mixing with the diluent on-board the instrument.
  • the packaging includes a cartridge reel adapted to contain a roll of the concentrate capsules retained in a concentrate tape configured to be dispensed from the cartridge reel. In this embodiment the concentrate tape includes two strips adhered to one another with the concentrate capsules sandwiched therebetween and adapted to be released from the concentrate tape.
  • an instrument utilising a reagent said instrument including:
  • a diluent chamber adapted to contain a diluent
  • a concentrate dispenser operatively coupled to the diluent chamber to dispense concentrate for mixing with the diluent on-board the instrument to produce the reagent at a required concentration.
  • the concentrate is contained in dissolvable capsules designed to dissolve during mixing with the diluent to produce the reagent.
  • the diluent is acidic or basic depending on the concentrate, and the dissolvable capsules are formed at least in part of a material which dissolves in the acidic or basic diluent.
  • the diluent chamber is a vacuum chamber to which the concentrate dispenser is operatively coupled wherein the concentrate is dispensed into the vacuum chamber with the assistance of vacuum pressure applied to the diluent chamber.
  • the concentrate dispenser includes a plunger for dispensing of the concentrate into the diluent chamber, preferably via a non-return valve.
  • the concentrate dispenser includes a frangible separator which cooperates with the diluent chamber wherein rupturing of the frangible separator effects dispensing of the concentrate to the diluent chamber.
  • the instrument is a laboratory instrument and the reagent is a high value reagent such as a molecular probe such as a nucleic acid probe or an antibody (Ab).
  • the concentrate may be in any state such as a liquid, solid, or lyophilised state.
  • the method may also comprise one or more subsequent steps of diluting the reagent with additional diluent to produce the required concentration.
  • packaging for use with an instrument in the on-board provision of a reagent, the packaging being adapted to contain a plurality of concentrate capsules, and configured to release each of the capsules for mixing with a diluent on-board the instrument to provide the reagent.
  • a container for use with an instrument in the on-board provision of a reagent the container adapted to contain a predetermined volume of a concentrate for mixing with a diluent on-board the instrument to provide the reagent.
  • a cover member for use with an instrument in the on-board provision of a reagent the cover member including a well being adapted to receive a concentrate for mixing with a diluent on- board the instrument to provide the reagent.
  • Figure 1 is a schematic of packaged concentrate dispensed into a cover member associated with a sample staining module (SSM) of an instrument having on-board production of the reagent according to an embodiment of one aspect of the invention;
  • SSM sample staining module
  • Figures 2(a) and 2(b) are schematics of alternative embodiments of mixing wells or chambers designed for on-board production of reagents
  • Figures 3(a) and 3(b) are schematics of alternative embodiments of chambers designed to be used in conjunction with the instrument of for example figure 1 ;
  • Figures 4(a) to 4(d) are schematics of different concentrate dispensers designed for the on-board provision of a reagent at an instrument according to embodiments of another aspect of the invention
  • Figures 5(a) to 5(c) are schematics of packaged concentrates/diluents used to produce reagents on-board an instrument according to embodiments of a further aspect of the invention. Detailed Description
  • FIG. 1 is a schematic illustration of a mixing well 10 associated with an instrument (not shown) for mixing a concentrate 12 with a diluent (not shown) on-board the instrument to provide a reagent at a required concentration.
  • the mixing well 10 is in this embodiment formed in a cover member 14 associated with a sample staining module (SSM) of the instrument.
  • the cover member 14 may be releasably attachable to the SSM of the instrument.
  • the mixing well in an alternative embodiment may be formed as an integral part of the instrument.
  • the instrument of this aspect of the invention is a laboratory instrument for treating a biological tissue sample within the SSM with the reagent, typically in the form of a molecular probe such as a nucleic acid probe or an antibody (Ab).
  • the high value reagent is produced at a desired concentration on-board the instrument by mixing the concentrate such as 12 and diluent to provide the reagent at the required concentration.
  • the concentrate 12 is provided in a sealed container 13.
  • the sealed container 13 includes a sealing membrane 18 arranged to contain the concentrate 12 within a plurality of sealed chambers 16.
  • the sealed container 13 of this example is in the form of a blister pack 20.
  • the blister pack 20 is designed to release each of the concentrate volumes such as 12 into the well 10 of the cover member 14.
  • the sealing membrane 18 which is in the form of a frangible foil is ruptured or otherwise broken or removed across an entry to the well 10 for release of the concentrate 12.
  • the diluent may be pumped from a bulk supply into the well 10 either before or after addition of the concentrate to achieve the required concentration.
  • the reagent is thus mixed and produced on-board the instrument.
  • the reagent may then be drawn under the cover member 14 or aspirated using a robot and a fluid transport probe (not shown) and then dispensed through a port 9 into a reaction area 1 1 for treatment, such as staining.
  • Figures 2(a) and 2(b) illustrate alternative embodiments suitable for production of a reagent on-board an instrument such as that including the cover member 14 of the previous embodiment of figure 1 .
  • the instrument is provided with multiple mixing wells 10A to 10D for serial dilution of the concentrate 12.
  • the reagent 12 is at stage 1 transferred to the mixing well 10B and at stage 2 diluted with diluent.
  • the resulting reagent is mixed in the mixing well 10B and at stage 3 transferred to mixing well 10C for further dilution at stage 4 with diluent.
  • the resulting reagent is mixed in mixing well 10C and at stage 5 transferred to mixing well 10D for further dilution with diluent at stage 6.
  • the final reagent at its required concentration is at stage 7 transferred from the mixing well 10D for use by the instrument.
  • the number of mixing wells required for each desired dilution may vary according to the required dilution. Accordingly, the number of mixing wells provided or utilized may vary according to the required dilution.
  • the final reagent may for example be used in staining a tissue sample located on a slide (not shown) of the SSM.
  • the multiple mixing wells 10A to 10D may be formed as an integral part of the instrument in for example the SSM or as shown in figure 1 fabricated in a fixed or disposable cover member of the SSM.
  • the instrument includes a probe 30 having an in-line mixing chamber 32.
  • the probe is for example in the form of a fluid transfer probe (FTP) of an instrument used for treating or staining tissue samples on slides.
  • FTP fluid transfer probe
  • the modified FTP 30 includes a diluent chamber 34 and a chamber 36 located up stream of the mixing chamber 32.
  • the diluent and chambers 34/36 provide the requisite volume of diluent 38 and concentrate 40 to the mixing chamber 32 to provide a reagent at the required concentration.
  • the FTP includes a nozzle 42 downstream of the mixing chamber 32 which is configured to dispense into a cover member of an SSM.
  • the nozzle 42 may discharge reagent directly on to the sample slide or into a port of a cover member such as 14 (see figure 1 ) associated with the SSM.
  • the instrument may incorporate a separate valve or valves (not shown) arranged on or adjacent to the mixing chamber.
  • Figures 3(a) and 3(b) are alternate embodiments of a chamber suitable for use with an instrument providing on-board production of a reagent.
  • the chambers may for example be suitable for use with the cover member 14 of the instrument of figure 1 .
  • the concentrate such as 12 is contained in a chamber 16 which is sealed with a sealing membrane 18.
  • the concentrate 12 is protected from evaporation and oxidation by the use of nitrogen or other inert gases 22 sealed within the chamber 16.
  • the sealing membrane 18 may be in the form of a foil pack or lid seal.
  • the embodiment of figure 3(b) is similar to the blister pack 20 of figure 1 having multiple chambers such as 16 in a common base plate 24.
  • FIG 4(a) to 4(d) illustrate different embodiments of a concentrate dispenser for use on-board an instrument in production of a reagent, for example the reagent being used in staining or otherwise treating tissue samples in an SSM of the instrument.
  • the embodiment of figure 4(a) schematically depicts mixing of a concentrate 12 with a diluent 13 to provide the reagent.
  • the concentrate 12 is in this embodiment contained in a dissolving capsule 15 designed to dissolve during mixing with the diluent 13.
  • the diluent 13 may be acidic or basic depending on the chemistry of the concentrate, and the capsule 15 formed of a material which dissolves in the diluent 13.
  • the diluent 13 may be contained in a mixing well associated with a cover member 14 of the SSM.
  • the concentrate such as 12 is contained in a concentrate dispenser 50 operatively coupled to an instrument for on-board provision of a reagent.
  • the concentrate dispenser 50 includes packaging 52 within which one of a plurality of the concentrate capsules such as 12A to 12F are contained in a stacked cartridge.
  • the stacked cartridge packaging 52 is designed to release each of the capsules such as 12A for mixing with a diluent on-board the instrument to provide a reagent at the required concentration.
  • the concentrate dispenser 50 includes a reciprocating release 54 operatively coupled to the stacked cartridge 52 to release a lowermost of the column of capsules such as 12A.
  • the packaging of the concentrate dispenser 50 is in the form of a cartridge reel 52.
  • the cartridge reel contains a roll of the concentrate capsules such as 12A to 12F retained in a concentrate tape 56 dispensed from the cartridge reel 52.
  • the concentrate tape 56 includes two strips 58A and 58B adhered to one another with the concentrate capsules such as 12F sandwiched therebetween.
  • the concentrate dispenser 50 of figure 4(c) also includes a spool 60 for removing the lower strip 58B of the concentrate tape 56 to release each of the concentrate capsules such as 12A from the dispenser 50.
  • the instrument includes a chamber 16 in the form of a disposable or reusable probe tip containing the concentrate 12.
  • the probe tip 16 is designed to fit to a probe such as 44 of the concentrate dispenser.
  • the probe may for example be in the form of a FTP of an instrument used in treating or staining tissue samples.
  • the probe tip 16 includes a nozzle 46 designed to cooperate with a port of for example a cover member of a SSM.
  • the nozzle 46 includes a temporary seal 48 which is designed to rupture on discharge of the concentrate 12 into the well for mixing with the diluent.
  • the concentrate 12 may also be sealed in the probe tip 16 with another seal 49 which is similarly ruptured under the application of pressure applied by the FTP 44.
  • Figures 5(a) to 5(c) illustrate various embodiments of a diluent chamber 17 operatively coupled to a concentrate dispenser 19 for mixing on-board an instrument to produce a reagent.
  • the diluent chamber is in the form of a mixing vial 17 with the concentrate dispenser 19 attached as a single package.
  • the diluent vial 17 has a vacuum pressure applied to it for dispensing of the concentrate 12 from the concentrate dispenser 19.
  • the concentrate dispenser 19 includes a plunger 21 for urging the concentrate 12 from the concentrate dispenser 19 into the diluent vial 17.
  • the concentrate dispenser 19 may include a one way valve 23 through which the concentrate 12 is discharged into the diluent vial 17.
  • the embodiment of figure 5(c) includes a concentrate dispenser in the form of the packaged chamber 16 such as the embodiments of figure 3(a).
  • the chamber 16 is operatively coupled to the diluent chamber or vial 17 with its sealing membrane 18 in contact with an entrance 25 to the diluent chamber 17.
  • the entrance 25 includes a spiked ridge 27 designed on the application of downward pressure to the chamber 16 to rupture the frangible sealing membrane 18.
  • the concentrate 12 is thus discharged into the diluent chamber 17 for mixing to produce the necessary reagent.
  • a concentrate includes liquids of varying concentrations and for example includes high-value reagents and bulk reagents.
  • the FTP of the earlier embodiment may thus extend to dispensing a reagent to be diluted, a diluent, other reagents, or a combination of these liquids.
  • the instrument in one embodiment may include a controller configured to implement the preferred method of producing a reagent on-board the instrument.
  • the method may be implemented via computer program code including instructions to control movement of a concentrate dispenser in, for example, dispensing a concentrate to a well of a cover member associated with a SSM.
  • the controller may also control dilution and mixing of the concentrate with a diluent to provide the reagent at the required concentration.
  • the concentration of the reagent produced on-board the instrument can be varied, for example, to achieve the required staining option for tissue samples;
  • On-board dilution improves laboratory workflow without having to pre-dilute reagents from concentrates and also reduces operator time and potential errors.

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  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Clinical Laboratory Science (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • General Health & Medical Sciences (AREA)
  • Physics & Mathematics (AREA)
  • Analytical Chemistry (AREA)
  • Biochemistry (AREA)
  • General Physics & Mathematics (AREA)
  • Immunology (AREA)
  • Pathology (AREA)
  • Biomedical Technology (AREA)
  • Molecular Biology (AREA)
  • Engineering & Computer Science (AREA)
  • Sampling And Sample Adjustment (AREA)

Abstract

La présente invention concerne de manière générale la production d'un réactif dans un instrument. L'instrument est pourvu d'un ou de plusieurs récipients de mélange (10) pour la dilution d'un concentré (12) avec un diluant afin d'obtenir le réactif à la concentration requise.
PCT/AU2013/001499 2012-12-21 2013-12-20 Procédé de production d'un réactif dans un instrument WO2014094062A1 (fr)

Priority Applications (3)

Application Number Priority Date Filing Date Title
EP13865320.9A EP2934730B1 (fr) 2012-12-21 2013-12-20 Procédé de production d'un réactif dans un instrument
US14/653,956 US20150343445A1 (en) 2012-12-21 2013-12-20 Method of producing a reagent on-board an instrument
US17/066,094 US20210121884A1 (en) 2012-12-21 2020-10-08 Method of producing a reagent on-board an instrument

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US201261745331P 2012-12-21 2012-12-21
US61/745,331 2012-12-21

Related Child Applications (2)

Application Number Title Priority Date Filing Date
US14/653,956 A-371-Of-International US20150343445A1 (en) 2012-12-21 2013-12-20 Method of producing a reagent on-board an instrument
US17/066,094 Continuation-In-Part US20210121884A1 (en) 2012-12-21 2020-10-08 Method of producing a reagent on-board an instrument

Publications (1)

Publication Number Publication Date
WO2014094062A1 true WO2014094062A1 (fr) 2014-06-26

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US (1) US20150343445A1 (fr)
EP (1) EP2934730B1 (fr)
WO (1) WO2014094062A1 (fr)

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* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US9927433B2 (en) * 2014-08-20 2018-03-27 Shin Corporation Test apparatus
JP2019512677A (ja) 2016-02-29 2019-05-16 ベンタナ メディカル システムズ， インコーポレイテッド 分注特徴付けのためのシステム及び方法

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EP2934730A4 (fr) 2016-11-23
EP2934730A1 (fr) 2015-10-28
US20150343445A1 (en) 2015-12-03

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